WO2016084169A1 - 内視鏡用シースおよび内視鏡用注射位置決め具 - Google Patents
内視鏡用シースおよび内視鏡用注射位置決め具 Download PDFInfo
- Publication number
- WO2016084169A1 WO2016084169A1 PCT/JP2014/081265 JP2014081265W WO2016084169A1 WO 2016084169 A1 WO2016084169 A1 WO 2016084169A1 JP 2014081265 W JP2014081265 W JP 2014081265W WO 2016084169 A1 WO2016084169 A1 WO 2016084169A1
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- Prior art keywords
- syringe
- passage
- distal end
- sheath
- proximal end
- Prior art date
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
- A61B1/012—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor characterised by internal passages or accessories therefor
- A61B1/018—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor characterised by internal passages or accessories therefor for receiving instruments
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/0067—Catheters; Hollow probes characterised by the distal end, e.g. tips
- A61M25/0082—Catheter tip comprising a tool
- A61M25/0084—Catheter tip comprising a tool being one or more injection needles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/06—Body-piercing guide needles or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/31—Details
- A61M5/32—Needles; Details of needles pertaining to their connection with syringe or hub; Accessories for bringing the needle into, or holding the needle on, the body; Devices for protection of needles
- A61M5/3287—Accessories for bringing the needle into the body; Automatic needle insertion
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
- A61B1/00064—Constructional details of the endoscope body
- A61B1/00071—Insertion part of the endoscope body
- A61B1/0008—Insertion part of the endoscope body characterised by distal tip features
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
- A61B1/00142—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with means for preventing contamination, e.g. by using a sanitary sheath
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/34—Trocars; Puncturing needles
- A61B17/3478—Endoscopic needles, e.g. for infusion
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/00234—Surgical instruments, devices or methods, e.g. tourniquets for minimally invasive surgery
- A61B2017/00292—Surgical instruments, devices or methods, e.g. tourniquets for minimally invasive surgery mounted on or guided by flexible, e.g. catheter-like, means
- A61B2017/0034—Surgical instruments, devices or methods, e.g. tourniquets for minimally invasive surgery mounted on or guided by flexible, e.g. catheter-like, means adapted to be inserted through a working channel of an endoscope
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/31—Details
- A61M5/32—Needles; Details of needles pertaining to their connection with syringe or hub; Accessories for bringing the needle into, or holding the needle on, the body; Devices for protection of needles
- A61M5/3287—Accessories for bringing the needle into the body; Automatic needle insertion
- A61M2005/3289—Accessories for bringing the needle into the body; Automatic needle insertion with rotation of the needle, e.g. to ease penetration
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/0067—Catheters; Hollow probes characterised by the distal end, e.g. tips
- A61M25/0082—Catheter tip comprising a tool
- A61M25/0084—Catheter tip comprising a tool being one or more injection needles
- A61M2025/0089—Single injection needle protruding axially, i.e. along the longitudinal axis of the catheter, from the distal tip
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/06—Body-piercing guide needles or the like
- A61M25/0662—Guide tubes
- A61M2025/0681—Systems with catheter and outer tubing, e.g. sheath, sleeve or guide tube
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/0067—Catheters; Hollow probes characterised by the distal end, e.g. tips
Definitions
- the present invention relates to an endoscope sheath and an endoscope injection positioning tool.
- an endoscope is inserted into the urethra, and a gel-like drug solution such as a collagen solution is injected inside the urethra wall using an injection needle to locally cover the urethra wall.
- a transendoscopic method of raising is used (for example, see Patent Document 1).
- the injection of the drug solution is usually performed at three places spaced in the circumferential direction by 120 °.
- Patent Document 1 discloses an endoscope sheath that is mounted on the outside of an endoscope so as to be rotatable about a longitudinal axis with respect to the endoscope. ing. A passage for the injection needle is formed through the side wall of the sheath in the longitudinal direction. By rotating the sheath relative to the endoscope, the puncture position of the injection needle protruding from the distal end of the sheath through the passage is rotated in the circumferential direction of the endoscope, and three injections are continuously performed. Can be done.
- the present invention has been made in view of the above-described circumstances, and can reliably prevent the injection needle from coming into contact with a portion other than the injection position of the tissue, and can easily provide a plurality of injection positions.
- An object of the present invention is to provide an endoscope sheath and an endoscope injection positioning tool that can be accurately determined.
- an elongate sheath body comprising an elongate rotating portion on the distal end side connected to be relatively rotatable about a longitudinal axis and a fixing portion on the proximal end side, and a proximal end surface from the distal end surface to the sheath body A first passage through which the insertion portion of the endoscope can be inserted, and a sheath body formed in parallel with the first passage from the distal end surface to the proximal end side.
- An outlet having an end portion withdrawn to the outside of the sheath body and a syringe having the injection needle that is provided in the fixing portion with a space in the circumferential direction around the longitudinal axis and that is withdrawn from the outlet A plurality of holding parts, wherein the holding parts are Fixing the syringe in the circumferential direction with respect to the fixing portion, the distal end of the shooting needle being arranged at the protruding position protruding from the distal end of the sheath body through the second passage, and more than the protruding position
- the proximal end of the syringe needle is released at a release position where the distal end of the injection needle is housed inside the sheath body, and the outlet is rotated in the state where the sy
- the sheath body is attached to the outside of the insertion portion by inserting the insertion portion of the endoscope into the first passage, and the insertion portion to which the sheath body is attached is inserted into the body.
- the tip of the injection needle protruding from the distal end of the sheath body is punctured into the tissue while observing with the endoscope, and the drug solution is injected can do.
- the needle tip is rotated and moved in the circumferential direction of the endoscope. Can be injected into another position spaced apart in the circumferential direction.
- the first injection is performed so that the direction around the longitudinal axis (rotational angle around the longitudinal axis) of the one holding part provided in the fixing part and the second passage is substantially the same.
- the direction around the longitudinal axis of the rotating part is determined, and the syringe is held in one holding part.
- the second injection the direction around the longitudinal axis of the rotating portion relative to the fixed portion is determined so that the orientation around the longitudinal axis of the other holding portion and the second passage is substantially the same.
- This is performed by holding the syringe in the holding part.
- the injection is performed a plurality of times while changing the holding portion for holding the syringe in the same manner. Thereby, it can inject to the position spaced apart in the circumferential direction according to the arrangement
- the drawing position of the proximal end portion of the injection needle drawn out from the drawing port to the outside of the sheath body in the radial direction is fixed as the direction of the rotating portion changes. It can be changed in the circumferential direction with respect to the part. Therefore, the holding part for holding the syringe can be changed by moving the released syringe in the circumferential direction with respect to the fixed part while the syringe needle is inserted into the second passage of the sheath body.
- the syringe when the syringe is held by the fixing portion and the needle tip of the injection needle is arranged at the protruding position protruding from the distal end of the sheath body, the syringe is fixed by the holding portion so as not to move in the circumferential direction of the fixing portion. Has been. Then, when the syringe is released from the holding portion by moving from the protruding position to the release position in order to move the syringe to another holding portion, the needle tip is retracted into the sheath body. Thereby, it is possible to prevent the injection needle from rotating inside the body while protruding from the sheath body, and to reliably prevent the injection needle from contacting a portion other than the injection position of the tissue.
- the distal end portion of the second passage may be inclined in a direction gradually separating from the longitudinal axis toward the distal end with respect to the longitudinal axis.
- the plurality of holding portions are provided in the fixing portion at intervals in the circumferential direction, open at a proximal end side, and at least a part of the syringe is from the proximal end side to the sheath body.
- You may have a some fitting hole which can be fitted in the substantially longitudinal direction. In this way, by sliding at least a part of the syringe from the proximal end side into the fitting hole, the syringe is held in the fitting hole so that the syringe does not move in the circumferential direction. The syringe can be released from the fitting hole by sliding the base end side.
- the fitting hole is between the maximum protruding position that restricts further movement of the syringe toward the distal end side and the retracted position that is proximal to the maximum protruding position.
- the syringe is held movably in the longitudinal direction, and the maximum protruding position is a position where the injection needle protrudes from the distal end of the sheath body by a predetermined length, and is between the maximum protruding position and the retracted position.
- the moving distance of the syringe may be greater than the predetermined length. In this way, the puncture depth of the injection needle into the tissue can be limited, and the injection needle can be reliably retracted inside the sheath body with the releasing operation of the syringe from the fitting hole. it can.
- the plurality of fitting holes are formed in a proximal end surface of the fixed portion, and the second portion is formed according to a relative angle between the rotating portion and the fixed portion around the longitudinal axis.
- the fixed portion is an arcuate or annular guide groove that connects the end portions on the front end side of the plurality of fitting holes, and a circumferential direction on the outer peripheral surface.
- a plurality of longitudinal grooves formed from the base end surface to the circumferential groove so as to connect the fitting holes and the circumferential groove to the outer circumferential surface.
- the guide groove, the circumferential groove and the plurality of longitudinal grooves have a width larger than the diameter of the injection needle, and the circumferential groove and the plurality of longitudinal grooves are larger than the diameter of the syringe. May have a small width.
- the syringe can be fitted into the fitting hole in accordance with the operation of inserting the injection needle into the second passage through the one fitting hole.
- the proximal end portion of the injection needle is moved from the fitting hole to the circumferential groove through the longitudinal groove, Is moved to another vertical groove, further moved from the other vertical groove to another fitting hole, and the syringe is fitted into the other fitting hole.
- the injection needle can be rotated and moved along the guide groove while extending substantially straight.
- the longitudinal groove and the circumferential groove that are narrower than the syringe restrict the pushing of the injection needle toward the distal end side. It is possible to reliably prevent the injection needle from protruding from the distal end of the sheath body during the movement.
- a first passage which is formed through the longitudinal axis from the distal end surface to the proximal end surface and capable of inserting an insertion portion of an endoscope, and the first passage from the distal end surface to the proximal end surface.
- An endoscope positioning tool formed in parallel with a passage and used in combination with an endoscope sheath having a second passage into which an injection needle can be inserted, the guide having a passage through which the insertion portion can be inserted At least a distal end portion of a syringe connected to a proximal end of an injection needle inserted into the second passage, the body being formed at a circumferentially spaced interval on the proximal end surface; It can be fitted in the central axis direction from the base end side, and is connected in the central axis direction alternatively to the second passage according to a relative angle around the longitudinal axis with the endoscope sheath.
- the guide groove, the circumferential groove and the plurality of longitudinal grooves have a width larger than the diameter of the injection needle, and the circumferential groove and the plurality of longitudinal grooves are An endoscope injection positioning tool having a width smaller than the diameter of the syringe.
- the present invention it is possible to surely prevent the injection needle from coming into contact with a portion other than the injection position of the tissue, and it is possible to easily and accurately determine a plurality of injection positions. .
- FIG. 1 is an overall configuration diagram of an injection kit for an endoscope including an endoscope sheath according to a first embodiment of the present invention.
- FIG. 2 is a cross-sectional view taken along the line II showing the configuration of a rotating part in the endoscope sheath of FIG. It is a longitudinal cross-sectional view which shows the shape of the 2nd channel
- FIG. 2 is a II-II transverse sectional view showing a configuration of a fixing portion in the endoscope sheath of FIG. It is a figure which shows the modification of the syringe used for the sheath for endoscopes of FIG.
- FIG. 7 is a hexahedral view illustrating a configuration of a fixing portion in the endoscope sheath of FIG. 6. It is a perspective view of the fixing
- an endoscope injection kit 100 according to a first embodiment of the present invention will be described with reference to FIGS. 1 to 5.
- an injection kit 100 according to this embodiment is used in combination with an endoscope for a urethra, and has a small-diameter hollow injection needle (syringe) connected to a syringe (syringe) 3. ) 1 and an endoscope sheath 2.
- the endoscope includes an elongated insertion portion that can be inserted into the urethra, and an operation portion connected to the proximal end of the insertion portion.
- the syringe 3 includes a cylindrical cylinder 3b that stores a chemical solution, and a piston 3c that is inserted into the cylinder 3b. By pressing the piston 3c, the chemical solution in the cylinder 3b is injected through the discharge port 3a. Supply into the needle 1 is possible.
- the drug solution is a solution that forms a gel at body temperature while flowing smoothly inside the injection needle 1, for example, a collagen solution.
- a cap portion 4 is provided at the proximal end portion of the injection needle 1, and is disposed on the distal end side of the syringe 3 and the syringe 3 in a state where the proximal end of the injection needle 1 is connected to the discharge port 3 a of the syringe 3.
- the cap portion 4 is fixed integrally.
- the endoscope sheath 2 includes an elongated sheath body 5 attached to the outside of the insertion portion of the endoscope, and three holding portions for holding the syringe 3 provided at a proximal end portion of the sheath body 5. 61, 62, 63.
- the sheath body 5 is divided into two bodies in the longitudinal direction, and includes a rotating portion 5A on the distal end side and a fixing portion 5B on the proximal end side.
- the rotating portion 5A has an elongated cylindrical shape that can accommodate substantially the entire length of the insertion portion.
- the rotating part 5A and the fixed part 5B are connected coaxially and connected so as to be relatively rotatable about the longitudinal axis A.
- FIG. 2 shows a cross section of the rotating portion 5A
- FIG. 4 shows a cross section of the fixed portion 5B.
- the sheath body 5 includes a first passage 7 and a second passage 8 that are formed in parallel with each other in the longitudinal direction.
- the first passage 7 is a passage for an insertion portion of an endoscope, and is a cylindrical space that is formed through the longitudinal axis A of the sheath body 5 from the distal end surface to the proximal end surface of the sheath body 5.
- the first passage 7 has an inner diameter that is slightly larger than the outer diameter of the insertion portion.
- the sheath body 5 and the insertion portion inserted into the first passage 7 from the proximal end side are in the longitudinal direction. Relative movement is possible and relative rotation about the longitudinal axis A is possible.
- the second passage 8 is a passage for the injection needle 1 and is formed in the longitudinal direction from the distal end surface of the sheath body 5 to the proximal end side on the radially outer side of the first passage 7.
- a needle introduction port (drawing outlet) 9 that opens radially outward is formed at the proximal end portion of the rotating portion 5 ⁇ / b> A, and the proximal end of the second passage 8 is connected to the needle introduction port 9.
- the second passage 8 has an inner diameter larger than the outer diameter of the injection needle 1, and the rotation portion 5 ⁇ / b> A and the injection needle 1 inserted into the second passage 8 from the needle introduction port 9 are in the longitudinal direction. The relative movement is possible. As shown in FIG.
- the tip portion of the second passage 8 constitutes an inclined portion 8a that is inclined with respect to the longitudinal axis A so as to gradually move away from the longitudinal axis A toward the tip of the rotating portion 5A.
- the angle formed between the inclined portion 8a and the longitudinal axis A is an angle suitable for puncturing the urethral wall of the injection needle 1, specifically, 30 ° to 40 °.
- the sheath body 5 has a water supply port 10 and a drain port 11 provided in the fixing portion 5B, and a liquid channel 12.
- the water supply port 10 communicates with the first passage 7, and the liquid (for example, cleaning liquid) injected from the water supply port 10 into the first passage 7 is inserted into the inner peripheral surface of the first passage 7 and the insertion portion. Is discharged from the opening of the distal end surface of the sheath body 5 through a gap between the outer peripheral surface and the outer peripheral surface of the sheath body 5.
- the liquid channel 12 is formed so as to penetrate from the distal end surface of the sheath body 5 to the drain port 11, and by sucking the liquid channel 12 from the drain port 11, the liquid in the vicinity of the distal end surface of the sheath body 5 is contained in the liquid channel 12. And is discharged from the drain port 11.
- each holding portion 61, 62, and 63 are provided on the outer peripheral surface of the fixed portion 5 ⁇ / b> B at three locations that are evenly spaced in the circumferential direction.
- Each holding portion 61, 62, 63 is a block-like member and has fitting holes 61 a, 62 a, 63 a that open on the radially outer side and the base end side of the sheath body 5.
- the fitting holes 61a, 62a, 63a are formed in a substantially longitudinal direction from the proximal end side to the distal end side of the sheath body 5, and are terminated at intermediate positions between the proximal ends and the distal ends of the holding portions 61, 62, 63. is doing.
- the fitting holes 61a, 62a, 63a have a shape that allows the convex portion 4a of the cap portion 4 to be fitted in the substantially longitudinal direction of the sheath body 5 from the proximal end side.
- the cap part 4 in which the convex part 4a is fitted in the fitting holes 61a, 62a, 63a and the syringe 3 fixed to the cap part 4 are fixed in the circumferential direction around the longitudinal axis A with respect to the fixing part 5B.
- further movement toward the tip side is restricted at the maximum protruding position (protruding position) where the convex portion 4a hits the inner wall at the end of the fitting holes 61a, 62a, 63a.
- the distal end portion of the injection needle 1 projects from the distal end surface of the sheath body 5 by a predetermined length d1. Further, the entire length of the injection needle 1 is designed. Further, the moving distance of the syringe 3 between the maximum projecting position and the retracted position where the convex portion 4a is located at the base end of the fitting holes 61a, 62a, 63a (see the two-dot chain line in FIG. 1) is d2. , The dimension in the longitudinal direction of the fitting holes 61a, 62a, 63a is designed so that d2 is larger than d1.
- the action of the injection kit 100 configured as described above will be described by taking the treatment of stress urinary incontinence as an example.
- the insertion portion of the endoscope is inserted into the first passage 7 of the sheath body 5 from the proximal end side.
- the sheath body 5 is attached to the insertion portion.
- the insertion part to which the sheath body 5 is attached is inserted into the urethra, and the distal end of the insertion part is positioned at an appropriate position in the urethra.
- the rotating portion 5A is fixed while the positions of the insertion portion and the fixing portion 5B are fixed so that the direction (rotation angle) around the longitudinal axis A of the needle introduction port 9 is substantially the same with respect to the one holding portion 61. Rotate.
- the injection needle 1 is inserted into the second passage 8 from the needle introduction port 9, and the cap portion 4 provided at the proximal end portion of the injection needle 1 that extends from the needle introduction port 9 to the outside of the sheath body 5.
- the syringe 3 is held by the holding portion 61 via the cap portion 4 by fitting the convex portion 4a into the fitting hole 61a. Then, when the syringe 3 is slid to the distal end side along the fitting hole 61a to the maximum projecting position, the distal end portion of the injection needle 1 can be projected from the distal end surface of the sheath body 5 by a predetermined length d1.
- the tip portion of the injection needle 1 can be observed by an endoscopic image.
- the distal end portion of the injection needle 1 is inclined at an angle of 30 ° to 40 ° with respect to the longitudinal axis A by the inclined portion 8 a provided at the distal end portion of the second passage 8. Projects diagonally forward to the outside. Therefore, the injection needle 1 can be punctured at an appropriate angle of 30 ° to 40 ° into the urethral wall adjacent to the side of the sheath body 5. Subsequently, the drug solution in the syringe 3 is injected from the tip of the injection needle 1 into the urethra wall. As a result, the urethral wall locally rises due to the medicinal solution injected inside the urethral wall.
- the syringe 3 is removed from the holding portion 61 by moving the syringe 3 to the base end side to a position (release position) where the convex portion 4a is arranged further to the base end side than the base end of the fitting hole 61a. .
- the syringe 3 is released from the holding portion 61 and is movable in the circumferential direction and the radial direction with respect to the fixed portion 5B.
- the moving distance d2 to the proximal end side of the syringe 3 necessary for removing the syringe 3 from the holding portion 61 is longer than the length d1 of the distal end portion of the injection needle 1 protruding from the distal end of the sheath body 5. Since it is large, the needle tip of the injection needle 1 is surely retracted inside the distal end of the sheath body 5 with the removal of the syringe 3 from the holding portion 61.
- the rotating portion 5A is held at 120 °. Rotate. And the syringe 3 is hold
- the syringe 3 is removed from the holding portion 62, and the positions of the insertion portion and the fixing portion 5B are fixed so that the direction around the longitudinal axis A of the needle introduction port 9 is substantially the same as the remaining holding portion 63.
- the rotating unit 5A is further rotated by 120 ° with the same.
- the syringe 3 is hold
- the medicinal solution can be injected into the urethra wall at three positions spaced by 120 ° in the circumferential direction.
- the syringe 3 does not move in the circumferential direction with respect to the fixed portion 5B between the maximum protruding position where the needle tip protrudes from the distal end surface of the sheath body 5 and the retracted position.
- the needle tip is reliably accommodated inside the sheath body 5. This prevents the injection needle 1 from rotating and moving in the urethra while being exposed from the sheath body 5, and ensures that the injection needle 1 contacts a site other than the injection position on the urethra wall. There is an advantage that can be prevented.
- each injection position is determined according to the circumferential position around the longitudinal axis A of the holding portions 61, 62, 63 that hold the syringe 3.
- the three injection positions are set to the three holding portions 61, 62, 63 in the fixing portion 5B. Similar to the arrangement, there is an advantage that it can be accurately and easily positioned at three positions spaced at equal intervals in the circumferential direction.
- the syringe 3 is held by the holding portions 61, 62, and 63 via the cap portion 4 that is integrally fixed to the syringe 3, but this is shown in FIG.
- the syringe 3 may be directly held by the holding portions 61, 62, 63 by fitting the convex portions 3d provided on the outer peripheral surface of the cylinder 3b into the fitting holes 61a, 62a, 63a.
- the convex portion 3d may be formed integrally with the cylinder 3b, or may be a member that can be attached to and detached from the cylinder 3b.
- an endoscope injection kit 100 according to a second embodiment of the present invention will be described with reference to FIGS.
- the injection kit 100 according to the present embodiment is different from the first embodiment mainly in the configuration of the fixing portion 5B ′ of the endoscope sheath 2. Therefore, in the present embodiment, the fixing portion 5B ′ will be mainly described, and the same components as those in the first embodiment are denoted by the same reference numerals and description thereof is omitted.
- FIG. 7A is a front view of the fixing portion 5B ′ viewed from the base end side
- FIG. 7B is a plan view
- FIG. 7C is a bottom view
- FIG. 7D is a left side view
- FIG. 7 Each shows a rear view.
- illustration of the water supply port 10 and the drain port 11 is omitted.
- the fixing portion 5B ′ is a cylindrical member, and includes three fitting holes (holding portions) 61a ′, 62a ′, 63a ′, a guide groove 5a, and a circumferential groove 5b.
- Three longitudinal grooves 5c are formed on the surface.
- the fitting holes 61 a ′, 62 a ′, 63 a ′ are formed on the base end face of the fixing portion 5 B ′ at three locations equally spaced in the circumferential direction, and the syringe 3 extends from the base end side in the longitudinal axis A direction.
- the tip portion of can be fitted.
- the fitting holes 61a ′, 62a ′, and 63a ′ are terminated at intermediate positions between the base end surface and the distal end surface of the fixing portion 5B ′, and the tip of the syringe 3 is fitted into the fitting holes 61a ′, 62a ′, and 63a.
- the distal end portion of the injection needle 1 projects by a predetermined length d1 from the distal end surface of the sheath body 5'. It is like that. Further, the syringe 3 is located between the maximum projecting position and the retracted position (see the two-dot chain line in FIG. 6) where the distal end of the syringe 3 is located at the proximal end of the fitting holes 61a ′, 62a ′, 63a ′.
- the longitudinal dimensions of the fitting holes 61a ′, 62a ′, and 63a ′ are designed so that d2 is larger than d1 when the moving distance is d2.
- the guide groove 5a is centered on the longitudinal axis A on the distal end surface of the fixed portion 5B ′ so as to connect the end portions on the distal end side of the three fitting holes 61a ′, 62a ′, 63a ′ in the circumferential direction. It is formed in a circular arc shape or an annular shape.
- the needle introduction port 9 is omitted, and the second passage 8 is formed through the longitudinal direction from the distal end surface to the proximal end surface.
- the radius of the guide groove 5a centered on the longitudinal axis A is substantially the same as the radial distance from the longitudinal axis A of the second passage 8 on the base end face of the rotating portion 5A.
- the three fitting holes 61a ′, 62a ′, 63a ′ alternatively rotate through the guide groove 5a according to the relative angle between the rotating portion 5A ′ around the longitudinal axis A and the fixed portion 5B ′.
- the second passage 8 of the part 5A ′ is continuous with the longitudinal direction.
- the circumferential groove 5b remains on the outer peripheral surface of the fixing portion 5B ′ from a position adjacent to the one fitting hole 61a ′ in the radial direction to a position adjacent to the other one fitting hole 63a ′ in the radial direction. It is formed in the circumferential direction via a position adjacent to the fitting hole 62a ′ in the radial direction.
- the longitudinal groove 5c is formed on the outer peripheral surface of the fixing portion 5B ′ in the longitudinal direction from the base end surface of the fixing portion 5B ′ to the peripheral groove 5b so as to connect the fitting holes 61a ′, 62a ′, 63a ′ to the peripheral groove 5b. Is formed.
- the width of the guide groove 5a, the circumferential groove 5b and the longitudinal groove 5c is designed to be larger than the outer diameter of the injection needle 1.
- the widths of the circumferential groove 5b and the vertical groove 5c are designed to be smaller than the outer diameter of the syringe 3.
- the method of using the endoscope sheath 2 according to the present embodiment is the first in the method of attaching the syringe 3 to the fixing portion 5B ′ and the method of moving the syringe 3 between the fitting holes 61a ′, 62a ′, 63a ′. Different from the embodiment.
- the insertion portion with the sheath body 5 ′ is inserted and positioned in the urethra,
- the rotating portion 5A ′ is rotated while the positions of the insertion portion and the fixing portion 5B ′ are fixed so that the direction around the longitudinal axis A of the second passage 8 is substantially the same with respect to the one fitting hole 61a ′.
- the injection needle 1 is inserted into the second passage 8 through the one fitting hole 61a ′ and the guide groove 5a, and the base of the injection needle 1 extending from the fitting hole 61a ′ to the outside of the sheath body 5 ′.
- the syringe 3 is held in the fitting hole 61a ′ by fitting the distal end portion of the syringe 3 connected to the end into the fitting hole 61a ′.
- the distal end portion of the injection needle 1 is projected from the distal end surface of the sheath body 5 ′ by a predetermined length d1, thereby causing the urethral wall. Is then punctured, and then the drug solution is injected inside the urethral wall.
- a position where the distal end of the syringe 3 is further arranged on the proximal side than the proximal end of the fitting hole 61a ′ ( The syringe 3 is removed from the holding portion 61 by moving the syringe 3 to the proximal end side until the release position.
- the moving distance d2 to the proximal end side of the syringe 3 necessary for removing the syringe 3 from the fitting hole 61a ′ is the length of the distal end portion of the injection needle 1 protruding from the distal end of the sheath body 5 ′. Since it is larger than d1, the needle tip of the injection needle 1 is reliably accommodated in the second passage 8 with the removal of the syringe 3 from the fitting hole 61a ′.
- the rotating portion Rotate 5A ′ by 120 °. Simultaneously with the rotation of the rotating portion 5A ', as shown in FIG. 8, the injection needle 1 connected to the syringe 3 is moved from the fitting hole 61a' to the circumferential groove 5b through the vertical groove 5c.
- the proximal end portion of the injection needle 1 is pulled out from the circumferential groove (drawing outlet) 5b to the outside in the radial direction of the sheath body 5 ′, and the drawing position of the injection needle 1 from the circumferential groove 5b is moved in the circumferential direction. Since the injection needle 1 and the syringe 3 can be moved in the circumferential direction with respect to the fixing portion 5B ′, the injection needle 1 is moved from the circumferential groove 5b to the fitting hole 62a ′ via another vertical groove 5c. Can do. Then, the syringe 3 is held in the fitting hole 62a ', and the second injection is performed on the urethral wall in the same manner as the first injection.
- path 7, the water supply port 10, and the drain port 11 is abbreviate
- the syringe 3 is removed from the fitting hole 62a ′, and the insertion portion and the fixing portion are arranged so that the direction around the longitudinal axis A of the second passage 8 is substantially the same as the remaining fitting hole 63a ′. While the position of 5B is fixed, the rotating unit 5A is further rotated by 120 °. Then, the syringe 3 is held in the fitting hole 63a ', and the third injection is performed on the urethral wall in the same manner as the first injection.
- the position of the syringe 3 is fixed by the narrow circumferential groove 5b and the vertical groove 5c. Since it is limited to the outside of ', the pushing of the injection needle 1 toward the distal end side is limited. Accordingly, there is an advantage that it is possible to more reliably prevent the injection needle 1 from being rotationally moved in the urethra while being exposed from the sheath body 5 '.
- Other effects of the present embodiment are the same as those of the first embodiment.
- the fixing portion 5B ′ described in the present embodiment alone may constitute an endoscope injection positioning tool.
- the water supply port 10 and the drain port 11 are unnecessary.
- the endoscope injection positioning tool is used in combination with a general-purpose endoscope sheath having the same structure as the rotating portion 5A or 5A ′, and attached to the insertion portion on the proximal end side with respect to the endoscope sheath. Even when a general-purpose endoscope sheath is used, the same effects as those of the first and second embodiments described above can be obtained.
Abstract
Description
本発明の第1の態様は、長手軸回りに相対回転可能に連結された先端側の細長い回転部と基端側の固定部とからなる細長いシース本体と、該シース本体に先端面から基端面まで前記長手軸に沿って貫通形成され、内視鏡の挿入部を挿入可能な第1の通路と、前記シース本体に先端面から基端側へ前記第1の通路と並列に形成され、注射針を挿入可能な第2の通路と、該第2の通路の基端と連通するとともに前記シース本体の半径方向外側において開口し、前記第2の通路内に挿入されている前記注射針の基端部分が前記シース本体の外側に引き出される引出口と、前記固定部に前記長手軸回りの周方向に間隔を空けて設けられ、前記引出口から引き出されている前記注射針を有する注射器を保持する複数の保持部とを備え、該保持部が、前記注射針の先端が前記第2の通路を介して前記シース本体の先端から突出する突出位置に配されている前記注射器を前記固定部に対して前記周方向に固定するとともに、前記突出位置よりも基端側の、前記注射針の先端が前記シース本体の内側に収納される解放位置において前記注射器を解放し、前記引出口は、前記注射器が前記保持部から解放されている状態において、前記回転部と前記固定部との相対回転に伴って、前記注射針の基端部分の引き出し位置を前記固定部に対して前記周方向に変更可能である内視鏡用シースである。
このようにすることで、注射針は、シース本体の先端から、内視鏡に対して半径方向外側へ向かって斜め前方に突出するので、シース本体の側方に位置する組織表面に対して注射針を斜めに穿刺することができる。
このようにすることで、注射器の少なくも一部分を基端側から嵌合穴内へスライドさせることによって、注射器が固定部に対して周方向に移動しないように嵌合穴に保持させ、また、注射器を基端側へスライドさせることによって注射器を嵌合穴から解放させることができる。
このようにすることで、注射針の組織への穿刺深さを制限することができるとともに、嵌合穴からの注射器の解放動作に伴って、注射針をシース本体の内側に確実に引っ込めることができる。
以下に、本発明の第1の実施形態に係る内視鏡用の注射キット100について、図1から図5を参照して説明する。
本実施形態に係る注射キット100は、図1に示されるように、尿道用の内視鏡と併用されるものであり、シリンジ(注射器)3に接続される細径で中空の注射針(注射器)1と、内視鏡用シース2とを備えている。
内視鏡は、尿道内に挿入可能な細長い挿入部と、該挿入部の基端に接続された操作部とを備えている。
シース本体5は、長手方向に2体に分割されており、先端側の回転部5Aと、基端側の固定部5Bとからなる。回転部5Aは、挿入部の長さ寸法の略全部を収容可能な細長い円筒状である。回転部5Aと固定部5Bとは、同軸に連結され、かつ、長手軸A回りに相対回転可能に連結されている。
本実施形態に係る注射キット100を使用して腹圧性尿失禁を治療するには、まず、内視鏡の挿入部をシース本体5の第1の通路7内に基端側から挿入することによって、シース本体5を挿入部に装着する。次に、シース本体5が装着されている挿入部を尿道内に挿入し、挿入部の先端を尿道内の適切な位置に位置決めする。次に、一の保持部61に対して針導入口9の長手軸A回りの向き(回転角度)が略同一となるように、挿入部および固定部5Bの位置を固定したまま、回転部5Aを回転させる。
続いて、シリンジ3内の薬液を注射針1の先端から尿道壁の内側へ注射する。これにより、尿道壁の内側に注射された薬液によって、尿道壁が局所的に隆起する。
以上により、周方向に120°の角度間隔を空けた3箇所において尿道壁に薬液を注射することができる。
次に、本発明の第2の実施形態に係る内視鏡用の注射キット100について、図6から図8を参照して説明する。
本実施形態に係る注射キット100は、図6に示されるように、主に、内視鏡用シース2の固定部5B’の構成において第1の実施形態と異なっている。したがって、本実施形態においては、固定部5B’について主に説明し、第1の実施形態と共通する構成については、同一の符号を付して説明を省略する。
図7に示されるように、固定部5B’は、円筒状の部材であり、3個の嵌合穴(保持部)61a’,62a’,63a’と、ガイド溝5aと、周溝5bと、3個の縦溝5cとがその表面に形成されている。
縦溝5cは、各嵌合穴61a’,62a’,63a’を周溝5bに接続するように、固定部5B’の外周面に、固定部5B’の基端面から周溝5bまで長手方向に形成されている。
本実施形態に係る内視鏡用シース2の使用方法は、シリンジ3の固定部5B’への取り付け方法および嵌合穴61a’,62a’,63a’間におけるシリンジ3の移動方法において、第1の実施形態と異なる。
本実施形態に係る注射キット100を使用して腹圧性尿失禁を治療するには、第1の実施形態と同様にして、シース本体5’を装着した挿入部を尿道内に挿入および位置決めし、一の嵌合穴61a’に対して第2の通路8の長手軸A回りの向きが略同一となるように、挿入部および固定部5B’の位置を固定したまま、回転部5A’を回転させる。
内視鏡用注射位置決め具を、回転部5Aまたは5A’と同様の構造を有する汎用の内視鏡用シースと併用し、内視鏡用シースよりも基端側において挿入部に装着することで、汎用の内視鏡用シースを用いた場合にも、上述した第1および第2の実施形態と同様の効果を得ることができる。
2 内視鏡用シース
3 シリンジ(注射器)
4 キャップ部
4a 凸部
5,5’ シース本体
5A,5A’ 回転部
5B 固定部
5B’ 固定部、内視鏡用注射位置決め具、本体
5a ガイド溝
5b 周溝(引出口)
5c 縦溝
61,62,63 保持部
61a,62a,63a,61a’,62a’,63a’ 嵌合穴(保持部)
7 第1の通路
8 第2の通路
8a 傾斜部分
9 針導入口(引出口)
10 給水口
11 排水口
12 液体チャネル
100 注射キット
Claims (6)
- 長手軸回りに相対回転可能に連結された先端側の細長い回転部と基端側の固定部とからなる細長いシース本体と、
該シース本体に先端面から基端面まで前記長手軸に沿って貫通形成され、内視鏡の挿入部を挿入可能な第1の通路と、
前記シース本体に先端面から基端側へ前記第1の通路と並列に形成され、注射針を挿入可能な第2の通路と、
該第2の通路の基端と連通するとともに前記シース本体の半径方向外側において開口し、前記第2の通路内に挿入されている前記注射針の基端部分が前記シース本体の外側に引き出される引出口と、
前記固定部に前記長手軸回りの周方向に間隔を空けて設けられ、前記引出口から引き出されている前記注射針を有する注射器を保持する複数の保持部とを備え、
該保持部が、前記注射針の先端が前記第2の通路を介して前記シース本体の先端から突出する突出位置に配されている前記注射器を前記固定部に対して前記周方向に固定するとともに、前記突出位置よりも基端側の、前記注射針の先端が前記シース本体の内側に収納される解放位置において前記注射器を解放し、
前記引出口は、前記注射器が前記保持部から解放されている状態において、前記回転部と前記固定部との相対回転に伴って、前記注射針の基端部分の引き出し位置を前記固定部に対して前記周方向に変更可能である内視鏡用シース。 - 前記第2の通路の先端部分が、前記長手軸に対して先端に向かって前記長手軸から漸次離間する方向に傾斜している請求項1に記載の内視鏡用シース。
- 前記複数の保持部は、前記固定部に前記周方向に間隔を空けて設けられ、基端側において開口して前記注射器の少なくとも一部分が基端側から前記シース本体の略長手方向に嵌合可能な複数の嵌合穴を有する請求項1または請求項2に記載の内視鏡用シース。
- 前記嵌合穴が、それ以上の前記注射器の先端側への移動を制限する最大突出位置と、該最大突出位置よりも基端側の後退位置との間で前記長手方向に移動可能に前記注射器を保持し、
前記最大突出位置は、前記注射針が前記シース本体の先端から所定の長さだけ突出する位置であり、
前記最大突出位置と前記後退位置との間の前記注射器の移動距離が、前記所定の長さよりも大きい請求項3に記載の内視鏡用シース。 - 前記複数の嵌合穴が、前記固定部の基端面に形成されるとともに、前記回転部と前記固定部との前記長手軸回りの相対角度に応じて前記第2の通路と択一的に前記長手方向に接続され、
前記固定部が、
前記複数の嵌合穴の先端側の端部同士を接続する円弧状または円環状のガイド溝と、
外周面に周方向に形成され前記引出口を構成する周溝と、
前記外周面に、各前記嵌合穴と前記周溝とを接続するように、前記基端面から前記周溝まで形成された複数の縦溝とを有し、
前記ガイド溝、前記周溝および前記複数の縦溝が、前記注射針の直径よりも大きな幅を有し、かつ、前記周溝および前記複数の縦溝が、前記注射器の直径よりも小さな幅を有する請求項3または請求項4に記載の内視鏡用シース。 - 先端面から基端面まで長手軸に沿って貫通形成され、内視鏡の挿入部を挿入可能な第1の通路と、先端面から基端面まで前記第1の通路と並列に形成され、注射針を挿入可能な第2の通路とを有する内視鏡用シースと併用される内視鏡用位置決め具であって、
前記挿入部を挿入可能な通路を有する略円筒状の本体を備え、
該本体が、
基端面に周方向に間隔を空けて形成され、前記第2の通路内に挿入されている注射針の基端に接続された注射器の少なくとも先端部分が基端側から中心軸方向に嵌合可能であり、前記内視鏡用シースとの前記長手軸回りの相対角度に応じて前記第2の通路と択一的に前記中心軸方向に接続される複数の嵌合穴と、
該複数の嵌合穴の先端側の端部同士を接続する円弧状または円環状のガイド溝と、
外周面に周方向に形成された周溝と、
前記外周面に、各前記嵌合穴と前記周溝とを接続するように、前記基端面から前記周溝まで形成された複数の縦溝とを有し、
前記ガイド溝、前記周溝および前記複数の縦溝が、前記注射針の直径よりも大きな幅を有し、かつ、前記周溝および前記複数の縦溝が、前記注射器の直径よりも小さな幅を有する内視鏡用注射位置決め具。
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DE112014007043.2T DE112014007043T5 (de) | 2014-11-26 | 2014-11-26 | Endoskophülle und Endoskop-Injektionspositioniervorrichtung |
PCT/JP2014/081265 WO2016084169A1 (ja) | 2014-11-26 | 2014-11-26 | 内視鏡用シースおよび内視鏡用注射位置決め具 |
CN201480083594.5A CN106998992A (zh) | 2014-11-26 | 2014-11-26 | 内窥镜用护套和内窥镜用注射定位器具 |
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JPWO2016084169A1 (ja) | 2017-09-21 |
CN106998992A (zh) | 2017-08-01 |
US20170252537A1 (en) | 2017-09-07 |
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